"hereditary disorders" trang 5 - tải miễn phí từ tailieuXANH
Ebook Liver pathology: Part 1

Ebook Liver pathology: Part 1
102    55    0
Ebook Neurological rehabilitation - Spasticity and contractures in clinical practice and research: Part 2

Ebook Neurological rehabilitation - Spasticity and contractures in clinical practice and research: Part 2
167    67    0
Reducing offline to online: an example and its applications

Reducing offline to online: an example and its applications
22    48    0
Ebook Breast cancer management for surgeons: Part 1

Ebook Breast cancer management for surgeons: Part 1
318    148    5
Ebook Breast cancer management for surgeons: Part 2

Ebook Breast cancer management for surgeons: Part 2
394    87    2
Retinoblastoma in a pediatric oncology reference center in Southern Brazil

Retinoblastoma in a pediatric oncology reference center in Southern Brazil
9    47    0
Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: A case report and review of the literature

Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: A case report and review of the literature
7    71    0
Temporal association between serious bleeding and immunization: Vitamin K deficiency as main causative factor

Temporal association between serious bleeding and immunization: Vitamin K deficiency as main causative factor
7    61    0
Chinese patient with neurofibromatosis-Noonan syndrome caused by novel heterozygous NF1 exons 1–58 deletion: A case report

Chinese patient with neurofibromatosis-Noonan syndrome caused by novel heterozygous NF1 exons 1–58 deletion: A case report
5    62    0
Broadening risk profile in familial colorectal cancer type X; increased risk for five cancer types in the national Danish cohort

Broadening risk profile in familial colorectal cancer type X; increased risk for five cancer types in the national Danish cohort
10    99    0
The first pancreatic neuroendocrine tumor in Li-Fraumeni syndrome: A case report

The first pancreatic neuroendocrine tumor in Li-Fraumeni syndrome: A case report
6    68    0
Targeted capture-based NGS is superior to multiplex PCR-based NGS for hereditary BRCA1 and BRCA2 gene analysis in FFPE tumor samples

Targeted capture-based NGS is superior to multiplex PCR-based NGS for hereditary BRCA1 and BRCA2 gene analysis in FFPE tumor samples
15    52    0
Comprehensive mutation detection of BRCA1/2 genes reveals large genomic rearrangements contribute to hereditary breast and ovarian cancer in Chinese women

Comprehensive mutation detection of BRCA1/2 genes reveals large genomic rearrangements contribute to hereditary breast and ovarian cancer in Chinese women
8    82    0
Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women

Investigating the effects of additional truncating variants in DNA-repair genes on breast cancer risk in BRCA1-positive women
12    58    0
Multiple intraneural glomus tumors in different digital nerve fascicles

Multiple intraneural glomus tumors in different digital nerve fascicles
5    56    0
BAP1 tumor predisposition syndrome case report: Pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy

BAP1 tumor predisposition syndrome case report: Pathological and clinical aspects of BAP1-inactivated melanocytic tumors (BIMTs), including dermoscopy and confocal microscopy
8    82    0
Germline BRCA1/BRCA2 mutations among high risk breast cancer patients in Jordan

Germline BRCA1/BRCA2 mutations among high risk breast cancer patients in Jordan
11    97    0
Variants of cancer susceptibility genes in Korean BRCA1/2 mutation-negative patients with high risk for hereditary breast cancer

Variants of cancer susceptibility genes in Korean BRCA1/2 mutation-negative patients with high risk for hereditary breast cancer
8    74    0
Prevalence of pathogenic BRCA1/2 germline mutations among 802 women with unilateral triple-negative breast cancer without family cancer history

Prevalence of pathogenic BRCA1/2 germline mutations among 802 women with unilateral triple-negative breast cancer without family cancer history
6    75    0
Pancreatic cancer as a sentinel for hereditary cancer predisposition

Pancreatic cancer as a sentinel for hereditary cancer predisposition
9    98    0
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